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2011
El-Karaksy, H., M. Fahmy, M. El-Raziky, N. El-Koofy, R. El-Sayed, M. S. Rashed, H. El-Kiki, A. El-Hennawy, and N. Mohsen, "Hereditary tyrosinemia type 1 from a single center in Egypt: clinical study of 22 cases.", World journal of pediatrics : WJP, vol. 7, issue 3, pp. 224-31, 2011 Aug. Abstract

BACKGROUND: Hereditary tyrosinemia type 1 (HT1) is an increasingly recognized inborn error of metabolism among Egyptian children. This study was undertaken to define the presenting clinical, biochemical and imaging features and outcome of 2-(2-motrp-4-trifluoromethylbenzoyl)-1, 3-cyclohexanedione (NTBC) therapy and liver transplantation in a cohort of Egyptian children diagnosed with HT1.

METHODS: The study was carried out at the Pediatric Hepatology Unit at Cairo University Children's Hospital. HT1 was diagnosed by quantification of succinylacetone (SA) in dry blood spots.

RESULTS: Twenty-two patients were diagnosed with HT1 in a period of 3 years from August 2006 to July 2009. Infants with focal hepatic lesions and hepatomegaly (n=13) were younger at diagnosis than those with rickets (n=5) (median age: 3.25 vs. 10 months; P=0.05). Alpha fetoprotein was highly elevated in all children. Seven children died within a few weeks of diagnosis before therapy was initiated. Ten children were treated with NTBC. The response to NTBC treatment was apparent by a steep drop in serum alpha fetoprotein (AFP) and undetectable SA in urine within 2 months. Three children underwent living donor liver transplantation after treatment with NTBC for 10, 18 and 22 months respectively, despite adequate response to therapy because of financial issues. The explanted livers were all cirrhotic with no dysplasia or malignant transformation.

CONCLUSIONS: Focal hepatic lesions are the commonest presentation of HT1 patients and they present at an earlier age than rickets. NTBC is effective but very expensive. Liver transplantation is still considered in HT1 patients.

El-Karaksy, H., M. Fahmy, M. El-Raziky, N. El-Koofy, R. El-Sayed, M. S. Rashed, H. El-Kiki, A. El-Hennawy, and N. Mohsen, "Hereditary tyrosinemia type 1 from a single center in Egypt: clinical study of 22 cases.", World journal of pediatrics : WJP, vol. 7, issue 3, pp. 224-31, 2011 Aug. Abstract

BACKGROUND: Hereditary tyrosinemia type 1 (HT1) is an increasingly recognized inborn error of metabolism among Egyptian children. This study was undertaken to define the presenting clinical, biochemical and imaging features and outcome of 2-(2-motrp-4-trifluoromethylbenzoyl)-1, 3-cyclohexanedione (NTBC) therapy and liver transplantation in a cohort of Egyptian children diagnosed with HT1.

METHODS: The study was carried out at the Pediatric Hepatology Unit at Cairo University Children's Hospital. HT1 was diagnosed by quantification of succinylacetone (SA) in dry blood spots.

RESULTS: Twenty-two patients were diagnosed with HT1 in a period of 3 years from August 2006 to July 2009. Infants with focal hepatic lesions and hepatomegaly (n=13) were younger at diagnosis than those with rickets (n=5) (median age: 3.25 vs. 10 months; P=0.05). Alpha fetoprotein was highly elevated in all children. Seven children died within a few weeks of diagnosis before therapy was initiated. Ten children were treated with NTBC. The response to NTBC treatment was apparent by a steep drop in serum alpha fetoprotein (AFP) and undetectable SA in urine within 2 months. Three children underwent living donor liver transplantation after treatment with NTBC for 10, 18 and 22 months respectively, despite adequate response to therapy because of financial issues. The explanted livers were all cirrhotic with no dysplasia or malignant transformation.

CONCLUSIONS: Focal hepatic lesions are the commonest presentation of HT1 patients and they present at an earlier age than rickets. NTBC is effective but very expensive. Liver transplantation is still considered in HT1 patients.

El-Karaksy, H., M. Fahmy, M. El-Raziky, N. El-Koofy, R. El-Sayed, M. S. Rashed, H. El-Kiki, A. El-Hennawy, and N. Mohsen, "Hereditary tyrosinemia type 1 from a single center in Egypt: clinical study of 22 cases.", World journal of pediatrics : WJP, vol. 7, issue 3, pp. 224-31, 2011 Aug. Abstract

BACKGROUND: Hereditary tyrosinemia type 1 (HT1) is an increasingly recognized inborn error of metabolism among Egyptian children. This study was undertaken to define the presenting clinical, biochemical and imaging features and outcome of 2-(2-motrp-4-trifluoromethylbenzoyl)-1, 3-cyclohexanedione (NTBC) therapy and liver transplantation in a cohort of Egyptian children diagnosed with HT1.

METHODS: The study was carried out at the Pediatric Hepatology Unit at Cairo University Children's Hospital. HT1 was diagnosed by quantification of succinylacetone (SA) in dry blood spots.

RESULTS: Twenty-two patients were diagnosed with HT1 in a period of 3 years from August 2006 to July 2009. Infants with focal hepatic lesions and hepatomegaly (n=13) were younger at diagnosis than those with rickets (n=5) (median age: 3.25 vs. 10 months; P=0.05). Alpha fetoprotein was highly elevated in all children. Seven children died within a few weeks of diagnosis before therapy was initiated. Ten children were treated with NTBC. The response to NTBC treatment was apparent by a steep drop in serum alpha fetoprotein (AFP) and undetectable SA in urine within 2 months. Three children underwent living donor liver transplantation after treatment with NTBC for 10, 18 and 22 months respectively, despite adequate response to therapy because of financial issues. The explanted livers were all cirrhotic with no dysplasia or malignant transformation.

CONCLUSIONS: Focal hepatic lesions are the commonest presentation of HT1 patients and they present at an earlier age than rickets. NTBC is effective but very expensive. Liver transplantation is still considered in HT1 patients.

Hamid, O. A., L. M. El Fiky, M. M. Medani, A. Abdelhady, and H. H. Ali, "Laryngeal cancer in Egypt: quality of life measurement with different treatment modalities.", Head & neck, vol. 33, issue 8, pp. 1162-9, 2011 Aug. Abstract

BACKGROUND: Quality of life (QOL) reflects the need to assess the patient's overall sense of well-being. A nonrandomized, prospective longitudinal study was conducted to evaluate QOL in Egyptian patients treated for laryngeal cancer.

METHODS: In all, 60 newly diagnosed patients with laryngeal cancer were divided into 3 groups: surgical resection, radiotherapy, and combined therapy. The European Organization for Research and Treatment of Cancer Quality of Life Questionnaires (EORTC-QLQ) were administered to the patients at 4 points: prior to treatment, during active treatment, and at 3 and 6 months after completion of treatment.

RESULTS: All pretreatment scales were worse in the combined therapy group. The functional scales reached their lowest levels in all groups during active treatment. Radiotherapy group scales showed persistent slow recovery. There was striking prevalence of the financial difficulties score in all groups.

CONCLUSION: QOL measurement provides information to guide clinical decision making in patients treated for laryngeal carcinoma.

Kassem, R. R., "Severe fibrosis of extraocular muscles after the use of lyophilized amniotic membrane in strabismus surgery.", Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus, vol. 15, issue 4, pp. 410, 2011 Aug. Abstract
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Abdallah, D. M., N. N. Nassar, and R. M. Abd-El-Salam, "Glibenclamide ameliorates ischemia-reperfusion injury via modulating oxidative stress and inflammatory mediators in the rat hippocampus.", Brain research, vol. 1385, pp. 257-62, 2011 Apr 18. Abstract

Stroke remains a debilitating disease with high incidence of morbidity and mortality, where many reports provide promising venues for prevention/treatment of such ailment. Glibenclamide, a selective blocker of KATP channels, was reported to protect against ischemia and ischemia-reperfusion (IR) injury in several experimental models. Hence, the present study aimed to investigate the possible involvement of free radicals as well as inflammatory and anti-inflammatory mediators in the hippocampus of rats exposed to IR. To this end, male Wistar rats were divided into 3 groups: group I served as sham operated controls; group II was subjected to 15 min ischemia by occlusion of both common carotid arteries, followed by 60 min reperfusion; group III was injected with glibenclamide (1mg/kg, i.p.) 10 min before ischemic-reperfusion injury. IR increased lipid peroxides, myeloperoxidase activity, TNF-α and PGE(2), while decreasing glutathione, total antioxidant capacity, nitric oxide and IL-10 levels in the hippocampus. Glibenclamide reversed all the former alterations, thus highlighting a potential therapeutic utility for this sulphonyl urea in IR brain injury via modulating oxidative stress and inflammatory mediators.

El-Shabrawi, M., H. El-Karaksy, N. Mohsen, M. Isa, M. Al-Biltagi, and M. El-Ansari, "Celiac disease in children and adolescents with autoimmune hepatitis: a single-centre experience.", Journal of tropical pediatrics, vol. 57, issue 2, pp. 104-8, 2011 Apr. Abstract

OBJECTIVES: Celiac disease (CD) is increasingly reported from North Africa, including Egypt. Autoimmune hepatitis (AIH) is considered a high risk factor for CD. We aimed to investigate the frequency of CD diagnosis in AIH.

METHODS: We prospectively enrolled 26 AIH patients aged 3.5-21 (mean 9.98 ± 3.94) years and 20 healthy age- and sex-matched controls. Serodiagnosis of CD was based on the most sensitive tests namely immunoglobulin A (IgA) human tissue transglutaminase antibody (IgA-tTGA) by enzyme-linked immunosorbent assay and/or IgA endomysial antibody (IgA-EMA) by immunofluoresence and confirmed the diagnosis by upper gastrointestinal endoscopy and histo-pathological findings in jejunal biopsy.

RESULTS: IgA-EMA was positive in four patients (15.4%), whereas IgA-tTGA was positive in two of them (7.7%). Histopathology was confirmatory in three (11.5%) seropositive patients.

CONCLUSION: The high prevalence (11.5%) of CD among Egyptian children with AIH indicates that CD exists in high-risk groups in our region and must be carefully looked into.

Geweely, N. S. I., "Evaluation of ozone for preventing fungal influenced corrosion of reinforced concrete bridges over the River Nile, Egypt.", Biodegradation, vol. 22, issue 2, pp. 243-52, 2011 Apr. Abstract

Fungal influenced corrosion (FIC) of some corroded sites in three selected bridges [Embaba bridge (E-bridge), Kasr al-Nile-bridge (K-bridge) and University bridge (U-bridge)] located over the River Nile in Egypt were investigated. Six fungal species, belong to 12 fungal genera, were isolated from the corroded reinforced concrete of the three tested bridges. Fourier transform infrared spectroscopy (FTIR) was screened for the most dominant fungal species (Fusarium oxysporium) which showed in all tested bridges that indicated the presence of amine group accompanied with polysaccharides contents. FIC of the most deteriorated bridge (K-bridge) was documented with FTIR. The association of fungal spores with corrosion products was recorded with scanning electron microscope (SEM). Evaluation of ozone for preventing FIC of the K-bridge was carried out by recording the corrosion rate and the corresponding inhibition efficiency (IE%). No mycelial growth with 100% IE was observed at 3 ppm ozone concentration after 120 min exposure time. With longer duration of ozone exposure, the membrane permeability of F. oxysporium was compromised as indicated by protein and nucleic acid leakages accompanied with lipid and tryptophan oxidation. The total intracellular and extracellular proteins of F. oxysporium were run on sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) indicated the increasing of the supernatant protein on the expense of the cellular protein bands with extending ozone exposure time (0-80 min).

Abou-Shady, O., M. S. El Raziky, M. M. Zaki, and R. K. Mohamed, "Impact of Giardia lamblia on growth, serum levels of zinc, copper, and iron in Egyptian children.", Biological trace element research, vol. 140, issue 1, pp. 1-6, 2011 Apr. Abstract

The aim of this study is to evaluate the serological levels of zinc, copper and iron in Giardia lamblia-infected children and to study the effect of giardiasis on their weight compared to controls. We studied 30 children, 1-10 years old, who attended the outpatient clinics of Cairo University Pediatric Hospital, with gastrointestinal complaints and diagnosed as having giardiasis by stools examination, they were enrolled as a study group. The control group consisted of 30 age- and sex-matched healthy children, free of gastrointestinal complaints and free of giardiasis. Serological levels of zinc, copper, and iron were measured by atomic absorption spectrophotometer. The infected group had significantly lower weight, serum iron, and zinc than controls (P = 0.035, <0.001, and <0.001 respectively) and 63.3% of patients infected with giardiasis were 1-5 years old. In the infected cases, 60% suffered from of abdominal pain, 50% from weight loss, and 40% had intermittent diarrhea. Infected cases with weight percentiles below the fifth had significantly lower serum iron than those with normal percentiles (>5th). In conclusion, most giardiasis-infected children were between 1 and 5 years, with significant affection of weight, abdominal pain, and/or intermittent diarrhea. Serum zinc and iron levels were significantly decreased in the infected group compared to control (P < 0.001).

El-Alfy, T. S., S. M. Ezzat, A. K. Hegazy, A. M. M. Amer, and G. M. Kamel, "Isolation of biologically active constituents from Moringa peregrina (Forssk.) Fiori. (family: Moringaceae) growing in Egypt.", Pharmacognosy magazine, vol. 7, issue 26, pp. 109-15, 2011 Apr. Abstract

BACKGROUND: Moringa peregrina is a wild plant that grown in the eastern desert mountains in Egypt. Although, this plant is native to Egypt, no details studies were traced on its chemical composition and biological activity.

MATERIALS AND METHODS: The different fractions of the ethanolic extract of the dried aerial parts of the plants were subjected to fractionation and purification on various silica and sephadex columns for the isolation of the major compounds which were tested for there anticancer activity. The aqueous and ethanolic extract as well as its different fractions were tested for antihyperglycemic effect on Streptozitocin-induced diabetes in rats.

RESULTS: Investigation of the different fractions of the ethanolic extract of the aerial parts of M. peregrina yielded lupeol acetate (1), β-amyrin (2), α-amyrin (3), β-sitosterol (4), β-sitosterol-3-O-glucoside (5), apigenin (6), rhamnetin (7), neochlorogenic acid (10), rhamnetin-3-O-rutinoside (12), and 6-methoxy-acacetin-8-C-β-glucoside (13) which were isolated for the first time from the plant. Compound (13) was isolated for the first time from genus Moringa. In addition, quercetin (8), chryseriol-7-O-rhamnoside (9) and quercetin-3-O-rutinoside (11) were also isolated. Identification has been established by spectral data (UV, MS, IR, 1H, 1H -1H COSY, and 13C-NMR). The major isolated compounds were found to have valuable cytotoxic activities against breast (MCF 7) and colon (HCT 116) cancer cell lines and their activities were comparable to the reference drug doxorubicin. On the other hand, the aqueous and ethanolic extracts as well as the n-hexane fraction were found to have potent antihyperglycemic effect on Streptozitocin-induced diabetes in rats.

CONCLUSION: The Egyptian plant M. peregrina is rich in biologically active ingredients which showed potent cytotoxic activity and also its ethanolic extraxt exert a significant antihyperglycemic effect.

Afifi, R. A. - R., D. K. Ali, and I. A. E. - M. Shaheen, "A localized case-control study of extra-gastric manifestations of Helicobacter pylori infection in children.", Indian journal of pediatrics, vol. 78, issue 4, pp. 418-22, 2011 Apr. Abstract

OBJECTIVE: To study extra- gastric manifestations of H. pylori infection among children in Egypt.

METHODS: This case-control study in which thirty [corrected] H pylori positive children were compared to thirty [corrected] H pylori negative children was conducted. Full history taking, clinical examination, CBC, serum iron, serum ferritin in addition to H pylori antibody testing were performed.

RESULTS: Mean hemoglobin, MCV, MCH, serum iron and serum ferritin were all less in seropositive patients but these were statistically non significant. Iron deficiency (ID) was defined as serum ferritin less than 12 ng/ml; and Iron deficiency anemia (IDA) as hemoglobin less than 11 g/dL in addition to ID. Seropositive patients showed increased frequency of ID and IDA and this was statistically significant (0.003 & 0.000 respectively). There was no statistically significant difference as regards the platelet counts of the two groups or the presence of skin disorders or the gender.

CONCLUSIONS: There is increased incidence of ID and IDA among H pylori positive children. This needs to be confirmed by larger therapeutic randomized controlled trials. The hematological response to eradication therapy needs to be further studied.

Anderson, B. O., E. Cazap, N. S. El Saghir, C. - H. Yip, H. M. Khaled, I. V. Otero, C. A. Adebamowo, R. A. Badwe, and J. B. Harford, "Optimisation of breast cancer management in low-resource and middle-resource countries: executive summary of the Breast Health Global Initiative consensus, 2010.", The lancet oncology, vol. 12, issue 4, pp. 387-98, 2011 Apr. Abstract

The purpose of the Breast Health Global Initiative (BHGI) 2010 summit was to provide a consensus analysis of breast cancer control issues and implementation strategies for low-income and middle-income countries (LMCs), where advanced stages at presentation and poor diagnostic and treatment capacities contribute to lower breast cancer survival rates than in high-income countries. Health system and patient-related barriers were identified that create common clinical scenarios in which women do not present for diagnosis until their cancer has progressed to locally advanced or metastatic stages. As countries progress to higher economic status, the rate of late presentation is expected to decrease, and diagnostic and treatment resources are expected to improve. Health-care systems in LMCs share many challenges including national or regional data collection, programme infrastructure and capacity (including appropriate equipment and drug acquisitions, and professional training and accreditation), the need for qualitative and quantitative research to support decision making, and strategies to improve patient access and compliance as well as public, health-care professional, and policy-maker awareness that breast cancer is a cost-effective, treatable disease. The biggest challenges identified for low-income countries were little community awareness that breast cancer is treatable, inadequate advanced pathology services for diagnosis and staging, and fragmented treatment options, especially for the administration of radiotherapy and the full range of systemic treatments. The biggest challenges identified for middle-resource countries were the establishment and maintenance of data registries, the coordination of multidisciplinary centres of excellence with broad outreach programmes to provide community access to cancer diagnosis and treatment, and the resource-appropriate prioritisation of breast cancer control programmes within the framework of existing, functional health-care systems.

El-Hamid, S. A., and W. El-Khayat, "Relationship of the protein Z intron F G79A and IL6 C634G gene polymorphisms with the risk of recurrent pregnancy loss in Egyptian women.", Journal of investigative medicine : the official publication of the American Federation for Clinical Research, vol. 59, issue 4, pp. 655-60, 2011 Apr. Abstract

PURPOSE: To investigate the relationship between recurrent pregnancy loss and single nucleotide polymorphisms in the protein Z (PZ) intron F G79A and the promoter region of the IL6 C634G genes in Egyptian women.

PROCEDURES: Single nucleotide polymorphisms in the PZ intron F G79A gene and the promoter region of the IL6 C634G gene were studied in 70 Egyptian women; 40 patients and 30 healthy and parous volunteers using the polymerase chain reaction-restriction fragment length polymorphism technique.

RESULTS: Regarding the PZ intron F G79A polymorphism; a higher prevalence of the A allele in the controls (53.3%) compared with the cases (22.5%) was found, and the difference proved to be statistically significant (P = 0.008). As for the IL6 C634G polymorphism, the frequency of the G allele was higher in the controls (100%) than in the cases (95%), but the difference did not prove to be statistically significant (P = 0.503). A statistically significant difference between the prevalence of the IL6 C634G (95%) and the PZ intron F G79A (22.5%) was detected (P ≤ 0.001).

CONCLUSION: A statistically significant difference of the frequency of the A allele of the PZ intron F G79A polymorphism was found with a higher prevalence of the A allele among the controls compared with the patients, suggesting a lower risk of recurrent pregnancy loss among the studied patients, but the IL6 C634G polymorphism did not prove to have an equivalent effect.

Al-Kappany, Y. M., M. R. Lappin, O. C. H. Kwok, S. A. Abu-Elwafa, M. Hilali, and J. P. Dubey, "Seroprevalence of Toxoplasma gondii and concurrent Bartonella spp., feline immunodeficiency virus, feline leukemia virus, and Dirofilaria immitis infections in Egyptian cats.", The Journal of parasitology, vol. 97, issue 2, pp. 256-8, 2011 Apr. Abstract

Toxoplasma gondii and Bartonella spp. are zoonotic pathogens of cats. Feline immunodeficiency virus (FIV) and feline leukemia virus (FeLv) are related to human immunodeficiency virus and human leukemia virus, respectively, and these viruses are immunosuppressive. In the present study, the prevalence of antibodies to T. gondii , Bartonella spp., FIV, as well as FeLv and Dirofilaria immitis antigens was determined in sera from feral cats (Felis catus) from Cairo, Egypt. Using a modified agglutination test, antibodies to T. gondii were found in 172 (95.5%) of the 180 cats with titers of 1∶5 in 9, 1∶10 in 9, 1∶20 in 3, 1∶40 in 5, 1∶80 in 5, 1∶160 in 15, 1∶320 in 22, and 1∶640 or higher in 104. Thus, 57.4% had high T. gondii titers. Antibodies to Bartonella spp. were found in 105 (59.6%) of 178, with titers of 1∶64 in 45, 1∶128 in 39, 1∶256 in 13, 1∶512 in 3, 1∶1,024 in 4, and 1∶2,048 in 1 cat. Antibodies to FIV were detected in 59 (33.9%) of 174 cats. Of 174 cats tested, antigens to FeLv, and D. immitis were detected in 8 (4.6%) and 6 (3.4%) cats, respectively. The results indicate a high prevalence of T. gondii, Bartonella spp., and FIV infections in cats from Cairo, Egypt. This is the first report of Bartonella spp., and D. immitis infection in cats in Egypt.

Othman, A. A., R. A. Lenz, J. Zhang, J. Li, W. M. Awni, and S. Dutta, "Single- and multiple-dose pharmacokinetics, safety, and tolerability of the selective alpha7 neuronal nicotinic receptor agonist, ABT-107, in healthy human volunteers.", Journal of clinical pharmacology, vol. 51, issue 4, pp. 512-26, 2011 Apr. AbstractWebsite

ABT-107 is a potent, selective α7 nicotinic receptor agonist under development for treatment of Alzheimer's disease and cognitive deficits associated with schizophrenia. The pharmacokinetics, safety, and tolerability of escalating single oral doses (1, 3, 10, 30, 60, 80, and 100 mg; double-blind, placebo-controlled, randomized, incomplete crossover design) and multiple oral doses (2, 6, and 15 mg once daily for 7 days; double-blind, placebo-controlled, randomized, parallel-group design) of ABT-107 were evaluated. Additionally, effect of food on ABT-107 pharmacokinetics (20-mg single dose) was evaluated using an open-label, 2-period, fasting and nonfasting, randomized, complete crossover design. ABT-107 exhibited nonlinear (more than dose-proportional) pharmacokinetics. ABT-107 half-life ranged from 7 to 10 hours, and steady state was achieved by day 6 of dosing. Food did not have a clinically meaningful effect on ABT-107 exposure. ABT-107 was safe and well tolerated over the tested dose range. The most frequently reported adverse events were nausea, headache, and tremor following single dosing and somnolence following multiple dosing. The pharmacokinetics, safety, and tolerability profiles of ABT-107 pose it as a good candidate for further development.

Fattouh, A. M., Y. A. Mansi, M. G. El-anany, A. A. El-kholy, and H. M. El-karaksy, "Acute lower respiratory tract infection due to respiratory syncytial virus in a group of Egyptian children under 5 years of age.", Italian journal of pediatrics, vol. 37, pp. 14, 2011. Abstract

BACKGROUND AND AIM: Respiratory syncytial virus (RSV) is one of the most important causes of acute lower respiratory tract infections (ALRTI) in infants and young children. This study was conducted to describe the epidemiology of ALRTI associated with RSV among children ≤ 5 years old in Egypt.

PATIENTS AND METHODS: We enrolled 427 children ≤ 5 years old diagnosed with ALRTI attending the outpatient clinic or Emergency Department (ED) of Children Hospital, Cairo University during a one- year period. Nasopharyngeal aspirates were obtained from the patients, kept on ice and processed within 2 hours of collection. Immunoflourescent assay (IFA) for RSV was performed.

RESULTS: 91 cases (21.3%) had viral etiology with RSV antigens detected in 70 cases (16.4%). The RSV positive cases were significantly younger than other non-RSV cases (mean age 8.2 months versus 14.2 months, p <0.001). RSV cases had significantly higher respiratory rate in the age group between 2-11 months (mean 58.4 versus 52.7/minute, p < 0.001) and no significant difference in the mean respiratory rate in the age group between 12-59 months. More RSV cases required supplemental oxygen (46% versus 23.5%, p < 0.001) with higher rate of hospitalization (37.1% versus 11.2%, p < 0.001) than the non-RSV cases. 97% of RSV cases occurred in winter season (p < 0.001).

CONCLUSION: RSV is the most common viral etiology of ALRTI in children below 5 years of age, especially in young infants below 6 months of age. It is more prevalent in winter and tends to cause severe infection.

Amer, A., H. Rakha, and I. El-Shawarby, "Agent-Based Behavioral Modeling Framework of Driver Behavior at the Onset of Yellow Indication at Signalized Intersections", 14th International IEEE Conference on Intelligent Transportation Systems (ITSC 2011), Washington, DC, Institute of Electrical and Electronics Engineers (IEEE), pp. 1809-1814, 2011. Abstract
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Amer, A., H. Rakha, and I. El-Shawarby, "Agent-Based Stochastic Modeling of Driver Decision at Onset of Yellow Light at Signalized Intersections", Transportation Research Record: Journal of the Transportation Research Board, vol. 2241, pp. 68-77, 2011. AbstractWebsite

This paper introduces two logistic statistical models for the driver stop-run decision at the onset of yellow at signalized intersections to capture the stochastic nature of the driver stop-run decision. One model is a classical frequentist model, whereas the other uses a Bayesian statistics approach. The Bayesian model parameters were calibrated by using the Markov Chain Monte Carlo slice procedure implemented within the MATLAB software. Both models were developed with 3,328 stop-run records, which were collected in a field experiment on the Virginia Smart Road, a limited-access highway between Blacksburg and Interstate 81 in Montgomery County, Virginia. The variables included in each model were driver gender, age, time to intersection, yellow time, approaching speed, and speed limit. Both models were shown to be consistent. For the Bayesian model application, two procedures were illustrated: cascaded regression and Cholesky decomposition. Both procedures produced replications consistent with the Bayesian model realizations, while these procedures captured the parameter correlations without the need to store the set of parameter realizations. The Bayesian model produced valid and transferable behavior by replicating multiple experimental results. The proposed Bayesian approach is ideal for modeling multiagent systems in which each agent has its own unique set of parameters.

Helmy, W., A. Kamel, and O. Hegazy, "Agile Software Development Methodologies", International Conference on Intelligent Computing and Information Systems, Cairo, Egypt, 2011.
Mohamadi, O., B. El-Hadidi, M. S. Bayoumi, and G. M. El-Bayoumi, "Analysis, and Implementation of a Sound Tracking System to Intercept a Moving Object", 14th International Conference on Aerospace science and Aviation Technology (ASAT), MTC, Cairo, Egypt, 2011.
El Shafei, H. I., "Anterolateral mini fronto-orbito-zygomatic craniotomy via an eyebrow incision in pediatrics: technical notes and evaluation.", Pediatric neurosurgery, vol. 47, issue 4, pp. 248-53, 2011. Abstract

BACKGROUND: Various approaches to lesions in the anterior cranial fossa and sellar region have been described by different authors under various names which describe the extent of craniotomies. The aims of this study were to describe and retrospectively analyze and evaluate the anterolateral mini fronto-orbito-zygomatic (MFOZ) approach via an eyebrow incision in treating pediatric pathologies, especially those related to the sellar region.

METHOD: Between January 2003 and December 2008, 18 patients with lesions in the sellar region or the anterior corridor leading to it were operated upon via the same approach. There were 10 males and 8 females. The age ranged between 11 months and 15 years (mean 7.9 years). The pathologies were craniopharyngiomas in 6 cases, hypothalamic and chiasmal pilocytic astrocytoma in 7 and 5 miscellaneous cases including 2 pituitary adenomas, 1 extradural hematoma, hypothalamic hamartoma and 1 arachnoid cyst in the retrosellar and prepontine area. Surgery was performed from the right side in 15 cases and from the left in 3 cases.

RESULTS: Total resection was achieved in 9 cases (50%), subtotal resection in 4 cases (22%), and partial resection in 5 cases (28%). Complications related to the approach like CSF rhinorrhea, supraorbital hypoesthesia and loss of upward elevation of the eyebrow were temporary. There was no mortality in this study and no significant added morbidities related to the approach. The approach has the advantages of the small cosmetic eyebrow incision and the skull base trajectory, thus reducing brain retraction and achieving the desired exposure with good outcome.

CONCLUSION: The MFOZ craniotomy using an eyebrow incision in pediatric patients is safe, effective, and both suitable and convenient for treating lesions especially at the sellar region.

Hossam M. Abdallah, Maha M. Salama, E. A. -elrahman S. E. - M. H. A., Antidiabetic activity of phenolic compounds from Pecan bark in streptozotocininduced diabetic rats, , vol. 4, issue 3, pp. 337 - 341, 2011. Abstract
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Torky, M., A. Mosharafa, A. Emran, A. Kamal, and M. Abdelhamid, "Antimicrobial therapy for asymptomatic patients with elevated prostate-specific antigen: can the change in prostate-specific antigen reliably guide prostate biopsy decisions?", Urologia internationalis, vol. 87, issue 4, pp. 416-9, 2011. Abstract

OBJECTIVES: To assess the effects of a 4-week levofloxacin course on PSA in asymptomatic men with elevated prostate-specific antigen (PSA) and on prostate biopsy decision.

METHODS: Fifty asymptomatic men with elevated PSA (4.0-10.0 ng/dl) were given levofloxacin 500 mg/day for 4 weeks followed by repeat PSA. Prostate biopsy was recommended at the end of the study. We compared pre- and post-treatment PSA as well as PSA changes between prostate cancer cases and non-cancer patients.

RESULTS: Mean (±SD) PSA decreased from 6.91 ± 2.13 to 6.05 ± 3.0 ng/dl after antimicrobial treatment (p = 0.025). Twenty-five (56.8%) patients had a post-treatment decrease in PSA, including 20 (45.5%) patients to <4.0 ng/dl and/or >25% of the initial PSA value. The difference in PSA change between prostate cancer and non-cancer patients was not statistically significant (p = 0.104).

CONCLUSIONS: Levofloxacin resulted in an overall decrease in PSA for asymptomatic men with PSA in the 4-10 ng/dl range. PSA changes, however, were not significantly different between patients with prostate cancer and non-cancer patients. Prostate cancer was detected in 20% of patients with a clinically relevant PSA decline.